JP2006232850A - Herbicide - Google Patents
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- JP2006232850A JP2006232850A JP2006119643A JP2006119643A JP2006232850A JP 2006232850 A JP2006232850 A JP 2006232850A JP 2006119643 A JP2006119643 A JP 2006119643A JP 2006119643 A JP2006119643 A JP 2006119643A JP 2006232850 A JP2006232850 A JP 2006232850A
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- RRKHIAYNPVQKEF-UHFFFAOYSA-P CC(c1c2c([SH+]c3nc(OC)cc(OC)n3)ccc1)OC2=[OH+] Chemical compound CC(c1c2c([SH+]c3nc(OC)cc(OC)n3)ccc1)OC2=[OH+] RRKHIAYNPVQKEF-UHFFFAOYSA-P 0.000 description 1
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/02—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
- A01N25/04—Dispersions, emulsions, suspoemulsions, suspension concentrates or gels
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/36—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< directly attached to at least one heterocyclic ring; Thio analogues thereof
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Abstract
Description
本発明は、新規液体除草製剤、その製造、及び栽培植物の収獲における不所望の植物の成長の制御における当該製剤の使用に関する。 The present invention relates to a novel liquid herbicidal formulation, its production and use of the formulation in controlling the growth of undesired plants in the harvest of cultivated plants.
本発明に従って、液体除草組成物(製剤)であって、慣用配合賦形剤に加えて、(a)非水性液相中に懸濁又は溶解された少なくとも1の雑草除草剤、(b)非水性液相中に懸濁された少なくとも1のスルホニルウレア型の除草剤、及び(c)少なくとも1の非イオン界面活性剤又はアニオン界面活性剤あるいは当該非イオン界面活性剤とアニオン界面活性剤の混合物を含むものが提案される。 In accordance with the present invention, a liquid herbicidal composition (formulation) comprising, in addition to conventional formulation excipients, (a) at least one weed herbicide suspended or dissolved in a non-aqueous liquid phase; At least one sulfonylurea type herbicide suspended in an aqueous liquid phase, and (c) at least one nonionic surfactant or anionic surfactant or a mixture of said nonionic surfactant and anionic surfactant. What is included is proposed.
本発明に従って使用されうる雑草除草剤は、特に、アセトアニリド、フェノキシプロピオン酸、ピリミジニルオキシ安息香酸、フェニルスルホニルトリアゾール、オキシアセトアミド、オキサゾリジンジオン、フェニルベンズアミド、ピリミジニル・チオフタリド及びインダンの化学種に属し、そして好ましくは、プレチラクロール、シハロフォップ、ピリミノバック、カフォンストロール、メフェナセット、フェントラザミッド、オキサジクロメフォン、ペントキサゾン、エトベンザニッド、インダノファン、並びにエポプロダン及び以下の式(I)の化合物: The weed herbicides that can be used according to the invention belong to the species of acetanilide, phenoxypropionic acid, pyrimidinyloxybenzoic acid, phenylsulfonyltriazole, oxyacetamide, oxazolidinedione, phenylbenzamide, pyrimidinyl thiophthalide and indane, and preferably Are pretilachlor, sihalofop, pyriminobac, cafonstrol, mefenacet, fentrazamid, oxadiclomephone, pentoxazone, etobenzanid, indanophan, and epoprodan and compounds of the following formula (I):
である。
上記雑草除草剤は、一緒に混合されて使用されることもできる。それらは、非水性液相中に溶解又は分散形態で存在する。上記スルホニルウレア型の除草剤も、好ましくは非水性液相中に分散される。これらは、好ましくは、シノスルフロン、ピラゾスルフロン、ベンスルフロン、アジムスルフロン、イマゾスルフロン、エトキシスルフロン、シクロスルファムロン又はハロスルフロンあるいはそれらの混合物である。
It is.
The above weed herbicides can also be used mixed together. They exist in dissolved or dispersed form in the non-aqueous liquid phase. The sulfonylurea type herbicide is also preferably dispersed in a non-aqueous liquid phase. These are preferably sinosulfuron, pyrazosulfuron, bensulfuron, azimusulfuron, imazosulfuron, ethoxysulfuron, cyclosulfamuron or halosulfuron or mixtures thereof.
好ましい非水性液相は、全ての植物油及び鉱油、例えば、ナタネ油、大豆油、ヒマワリ油、ヒマシ油、マツ(pine)油、綿実油、並びにこれらの油の誘導体、例えば、エステル、特にこれらの油のメチルエステル、並びにパラフィン及び芳香族鉱油、例えば、Orchex796,Shellsolタイプ、Isoparタイプ、芳香族画分、例えば、Solvesso200、及びエステル、例えば、Exxate700、並びにそれらの混合物を含む。 Preferred non-aqueous liquid phases are all vegetable and mineral oils such as rapeseed oil, soybean oil, sunflower oil, castor oil, pine oil, cottonseed oil, and derivatives of these oils such as esters, especially these oils Methyl esters, as well as paraffin and aromatic mineral oils such as Orchex 796, Shellsol type, Isopar type, aromatic fractions such as Solvesso 200, and esters such as Exxate 700, and mixtures thereof.
上記非イオン及びアニオン界面活性剤は、慣用の、商業的に入手可能な物質、例えば、エトキシル化植物油、Emulsogen EL、エトキシル化脂肪アルコール、例えば、Genapol O−050、エトキシル化アルキルフェノール、例えば、Synperonic NP8、エトキシル化ポリエチレン・グリコール又はポリプロピレン・グリコール、例えば、Pluronic型、エトキシル化トリスチリルフェノール誘導体、例えば、Soprophor 4D384又はSoprophor S/25、オレイル・ポリグリコール・エーテル、例えば、Genapol U−050、及びシリコーン界面活性剤、例えば、Silwet L77、並びにドデシルベンゼン・スルホネート、例えば、Sermul 88A、アルコール・エーテル・スルホネート、例えば、Genapol LRO、リグニン・スルホネート、例えば、Ultrazin NA、フェノール・スルホネート、例えば、Sipragil GN及びポリカルボキシレート、例えば、Geropon TA72、スルホネート化ナフタレン/ホルムアルデヒド濃縮物、例えば、Supragil MSN、スルホスクシネート、例えば、Aerosol OT70PG、ポリアクリレート誘導体、例えば、Atlox 4913、マレイン酸/オレフィン・コポリマー、例えば、Sokolan CP9、アルキル・ポリグリコシド、アルキル無水コハク酸誘導体、ソルビタン・エステル、エトキシル化ソルビタン・エステル、アルキル及びアルキルアリール・ポリグリコール・エーテル・リン酸エステル及びエトキシル化脂肪酸エステル、並びにタウリド(taurides)、例えば、Hostapon T hk であることができる。 The nonionic and anionic surfactants are conventional, commercially available materials such as ethoxylated vegetable oils, Emulsogen EL, ethoxylated fatty alcohols such as Genapol O-050, ethoxylated alkylphenols such as Synperonic NP8. Ethoxylated polyethylene glycols or polypropylene glycols such as Pluronic type, ethoxylated tristyrylphenol derivatives such as Soprophor 4D384 or Soprophor S / 25, oleyl polyglycol ethers such as Genapol U-050, and silicone interfaces Activators such as Silwet L77, as well as dodecylbenzene sulfonates such as Sermul 88A, alcohol Ether ether sulfonates such as Genapol LRO, lignin sulfonates such as Ultrazin NA, phenol sulfonates such as Sipragil GN and polycarboxylates such as Geron TA72, sulfonated naphthalene / formaldehyde concentrates such as Supragil MSN Sulfosuccinates such as Aerosol OT70PG, polyacrylate derivatives such as Atlox 4913, maleic acid / olefin copolymers such as Sokolan CP9, alkyl polyglycosides, alkyl succinic anhydride derivatives, sorbitan esters, ethoxylated sorbitans・ Ester, alkyl and alkyl aryl ・ Polyglycol ・ Ether ・ Phosphate Tellurium and ethoxylated fatty acid esters, and taurides, such as Hostapon Thkh.
上述の除草剤は、the Pesticide Manual,Eleventh Edition,British Crop Protection Council,1997中に記載されている。式(I)の化合物は、EP−A−447506から知られ、フェントラザミッドはBritish Crop Protection Conference Proceedings,1997,67−72から知られ、そしてオキサジクロメフォンは、British Crop Protection Conference Proceedings,1997,73−80から知られている。 The above-mentioned herbicides are described in the Pesticide Manual, Eleventh Edition, British Crop Protection Council, 1997. Compounds of formula (I) are known from EP-A-447506, fentrazamid is known from British Crop Protection Conference Proceedings, 1997, 67-72, and oxadichrome mefone is from British Crop Protection Conference Proceedings, 1997 73-80.
本発明に係る好ましい除草製剤は、雑草除草剤として、シハロフォップ(cyhalofop)、ピリミノバック(pyriminobac)、キャフェンストロール(cafenstrole)、メフェナセット(mefenacet)、フェントラザミド(fentrazamid)、オキサジクロメフォン(oxaziclomefon)、ペントキザゾン(pentoxazone)、エトベンザニッド(etobenzanid)、インダノファン(indanofan)、エポプロダン(epoprodan)、プレチラクロール(pretilachlor)、又は以下の式(I): Preferred herbicidal preparations according to the present invention include, as weed herbicides, cyhalofops, pyriminobac, fenfentrol, mefenacet, fentrazamide, oxadiclomephone, (Pentoxazole), etobenzanid, indanophan, epoprodan, pretilachlor, or the following formula (I):
により表される化合物、あるいはその混合物を含む。請求項1記載の製剤。
前記スルホニルウレア型の除草剤として、本発明に係る製剤は、好ましくは、ピラゾスルフロン(pyrazosulfuron)、ベンスルフロン(bensulfuron)、アジムスルフロン(azimsulfuron)、イマゾスルフロン(imazosulfuron)、エトキシスルフロン(ethoxysulfuron)、シクロスルファムロン(cyclosulfamuron)、ハロスルフロン(halosulfuron)又はシノスルフロン(cinosulfuron)又はその混合物を含む。
Or a mixture thereof. The formulation according to claim 1.
As the sulfonylurea type herbicide, the preparation according to the present invention is preferably pyrazosulfuron, bensulfuron, azimsulfuron, imazosulfuron, ethoxysulfuron, ethoxysulfuron. Including cyclosulfuron, halosulfuron, cinosulfuron or mixtures thereof.
使用される非水性液相は、好ましくは、植物油又は鉱油あるいはこれらの油の混合物である。
考えうる好ましい非イオン界面活性剤は、エトキシル化植物油、エトキシル化脂肪アルコール、エトキシル化アルキルフェノール、エトキシル化ポリエチレン・グリコール又はポリプロピレン・グリコールあるいはそれらのコポリマー、エトキシル化トリスチリルフェノール誘導体、オレイル・ポリグリコール・エーテル又はシリコーン界面活性剤を含み、そしてアニオン界面活性剤は、ドデシルベンゼン・スルホネート、スルホスクシネート、エトキシル化トリスチリルフェノール・スルフェート又はホスフェート、アルコール・エーテル・スルホネート、リグニン・スルホネート、エトキシル化フェノール・スルフェート又はポリカルボキシレートであることができる。
The non-aqueous liquid phase used is preferably a vegetable or mineral oil or a mixture of these oils.
Possible preferred nonionic surfactants are ethoxylated vegetable oils, ethoxylated fatty alcohols, ethoxylated alkylphenols, ethoxylated polyethylene glycols or polypropylene glycols or copolymers thereof, ethoxylated tristyrylphenol derivatives, oleyl polyglycol ethers Or a silicone surfactant and the anionic surfactant is dodecylbenzene sulfonate, sulfosuccinate, ethoxylated tristyrylphenol sulfate or phosphate, alcohol ether sulfonate, lignin sulfonate, ethoxylated phenol sulfate Or it can be a polycarboxylate.
重要な製剤は、前記雑草除草剤として、植物油中に懸濁又は溶解されたプレチラクロール(pretilachlor)又は式(I)の化合物あるいはそれらの混合物を、前記スルホニルウレア型の除草剤として、植物油中に懸濁されたベンスルフロン(bensulfuron)、ピラゾスルフロン(pyrazosulfuron)、アジムスルフロン(azimsulfuron)、イマゾスルフロン(imazosulfuron)又はシノスルフロン(cinosulfuron)あるいはそれらの混合物を、そして前記界面活性剤として、非イオン化合物とアニオン化合物の混合物を含むものである。 An important formulation is a pretilachlor or a compound of formula (I) or a mixture thereof suspended or dissolved in vegetable oil as the weed herbicide, suspended in vegetable oil as the sulfonylurea type herbicide. Benzosulfuron, pyrazosulfuron, azimsulfuron, imazosulfuron or sinosulfuron or a mixture of these as a nonionic surfactant, and a nonionic surfactant as a compound, Is included.
これらの中で、好ましいのは、前記雑草除草剤として、植物油中に懸濁又は溶解された式(I)の化合物、前記スルホニルウレア型の除草剤として、植物油中に懸濁されたシノスルフロン(cinosulfuron)そして、界面活性剤として、非イオン化合物とアニオン化合物の混合物を含む製剤である。
これらの中で、さらに好ましいのは、前記雑草除草剤として、植物油中に懸濁又は溶解されたプレチラクロール(pretilachlor)、前記スルホニルウレア型の除草剤として植物油中に懸濁された、シノスルフロン(cinosulfuron)、そして界面活性剤として、非イオン化合物とアニオン化合物の混合物を含む製剤である。
Among these, preferred is the compound of formula (I) suspended or dissolved in vegetable oil as the weed herbicide, and cinosulfuron suspended in vegetable oil as the sulfonylurea type herbicide. And it is a formulation containing the mixture of a nonionic compound and an anionic compound as surfactant.
Among these, more preferred as the weed herbicide is pretilachlor suspended or dissolved in vegetable oil, and sinosulfuron suspended in vegetable oil as the sulfonylurea type herbicide, And it is a formulation containing a mixture of a nonionic compound and an anionic compound as a surfactant.
特に有効な製剤は、前記雑草除草剤として、ナタネ油又はナタネ油メチル・エステルあるいはそれらの混合物中に懸濁又は溶解された、プレチラクロール又は式(I)の化合物あるいはそれらの混合物を、前記スルホニルウレア型の除草剤として、ナタネ油又はナタネ油メチル・エステルあるいはそれらの混合物中に懸濁されたベンスルフロンを、そして前記界面活性剤として、ヒマシ油エトキシレート、ドデシルベンゼン・スルホネート、エトキシル化トリスチリルフェノール・スルフェート及びオレイル・ポリグリコール・エーテルから選ばれる、非イオン化合物とアニオン化合物の混合物を含む。 A particularly effective formulation is the sulfonylurea-type compound of pretilachlor or a compound of formula (I) or a mixture thereof suspended or dissolved in rapeseed oil or rapeseed oil methyl ester or a mixture thereof as the weed herbicide. As a herbicide, rapeseed oil or rapeseed oil methyl ester or a mixture thereof, bensulfuron, and as the surfactant, castor oil ethoxylate, dodecylbenzene sulfonate, ethoxylated tristyrylphenol, Includes a mixture of nonionic and anionic compounds selected from sulfate and oleyl polyglycol ether.
本発明に係る製剤は、それらが高濃度で除草活性成分を含有することができ、かつ、それらが長い時間にわたり分解から保護されて残存するという大きな利点をもつ。それらは、他の油溶性又は液体混合物、例えば、生物学的活性を高めるために好適な添加物、並びに安定剤、例えばエポキシド化した植物油が、問題を伴わずに添加されることができるという可能性をも提供する。驚ろくべきことに、本発明に係る製剤は、有機液体の使用に拘らず、それらの適用後に栽培植物の収獲に対して実際上の害を及ぼさない。 The formulations according to the invention have the great advantage that they can contain herbicidal active ingredients in high concentrations and that they remain protected from degradation for a long time. They allow other oil-soluble or liquid mixtures, such as additives suitable for enhancing biological activity, as well as stabilizers, such as epoxidized vegetable oils, can be added without problems. It also provides sex. Surprisingly, the preparations according to the invention have no practical harm to the harvest of cultivated plants after their application, regardless of the use of organic liquids.
本発明に係る製剤は、好ましくは、水をはった水田における雑草の防除のために好適である。本法は、有利には、要求量の製剤が等量〜10倍量の水と混合され、そして既に水をはった水田に直接適用され、又は水田の水はりの間に流入する水に添加される(いわゆる、放出(splash)適用)ようなやり方で行われる。さらに、稲の機械による植え付けと同時に、上記製剤を適下して又は部分として適用することもできる(いわゆる、浸漬(dip)適用)。 The preparation according to the present invention is preferably suitable for controlling weeds in paddy fields with water. The method is advantageously applied to water flowing directly between paddy fields, where the required amount of the formulation is mixed with an equal amount to 10 times the amount of water and applied directly to the paddy field. It is carried out in such a way that it is added (so-called splash application). Furthermore, simultaneously with planting of rice, the preparation can also be applied as a part or part (so-called dip application).
本発明に係る製剤のスプレー適用も同様に可能であるが、水によるより高い希釈を要求する。
本発明に係る製剤の適用割合は、広いレンジ内で変化しうる。50〜2000g/haの除草剤を使用することが好ましい(雑草除草剤プラススルホニルウレア型の除草剤)。
Spray application of the formulation according to the invention is possible as well, but requires a higher dilution with water.
The application rate of the formulation according to the invention can vary within a wide range. It is preferable to use 50 to 2000 g / ha of herbicide (weed herbicide plus sulfonylurea type herbicide).
本発明に係る液体製剤は、1リッター当り、30〜1920gの雑草除草剤及び20〜80gのスルホニルウレア型の除草剤、並びに50〜300gの界面活性剤(アニオン・プラス・非イオン)を含む。通常、2〜20l/haの、以下実施例に記載する配合物が、直接適用又は放出適用のために要求される。放出適用のためには、この量は、通常20〜500l/haである。本発明に係る製剤は、さらなる慣用添加物、例えば、不活性担体、例えば、カオリン(kaolin)及びチョーク(chalk)、安定剤、消泡剤、保存料、粘度調節剤、増粘剤、例えば、ケイ酸又はベントナイト、バインダー、粘着剤(tackifier)、並びに肥料又は他の活性成分を含むこともできる。上記製剤は、知られたやり方で、例えば、上記活性成分を上記配合賦形剤及び液体又は固体担体とじかに混合し、そして/又はそれとともに粉砕することにより製造される。 The liquid preparation according to the present invention contains 30 to 1920 g of weed herbicide and 20 to 80 g of sulfonylurea type herbicide and 50 to 300 g of surfactant (anion plus nonion) per liter. Usually 2 to 20 l / ha of the formulation described in the examples below is required for direct or release application. For release applications, this amount is usually 20 to 500 l / ha. The preparations according to the invention are further customary additives such as inert carriers, such as kaolin and chalk, stabilizers, antifoams, preservatives, viscosity modifiers, thickeners, for example It may also contain silicic acid or bentonite, binders, tackifiers, and fertilizers or other active ingredients. The formulations are prepared in a known manner, for example by mixing the active ingredient directly with the formulation excipient and liquid or solid carrier and / or grinding with it.
特に好ましい配合物は、以下のように調製される:
配合実施例
A particularly preferred formulation is prepared as follows:
Example of formulation
適用実施例
配合物F1,F2,F3,F4,F5,F6,F7,F8,F9及びF10を水で5lに希釈し、そして5l/haの適用割合で水をはった水田に直接導入する(放出適用)。適用後22日目に、雑草、エキノクロア(Echinochloa)、シルパス(Scirpus)、及びモノコリア(Monochoria)の防除、並びに稲に対する上記製剤の植物毒性活性を調べる(100%は、雑草の完全な防除又は完全に枯れた稲を示し、0%は雑草の防除が全くないこと又は稲に対する植物毒性活性が全くないことを示す)。これは、エキノクロアの並行して行われる、a)発芽の間、b)2.5葉段階における、そしてc)4.1葉段階における、テストにおいて生じる。上記テストにおいて得られた結果を以下の表に要約する:
Application Examples Formulations F1, F2, F3, F4, F5, F6, F7, F8, F9 and F10 are diluted to 5 liters with water and introduced directly into the paddy field with water at an application rate of 5 liters / ha. (Release application). On the 22nd day after application, control of weeds, Echinochloa, Sirpus, and Monochoria, and the phytotoxic activity of the formulation against rice (100% is considered to be complete or complete control of weeds) And 0% indicates no weed control or no phytotoxic activity against rice). This occurs in tests performed in parallel with echinochlor, a) during germination, b) at the 2.5 leaf stage, and c) at the 4.1 leaf stage. The results obtained in the above test are summarized in the following table:
上記配合物が、例えば、2〜500lまで水で希釈される場合に、同じ結果が得られる。 The same result is obtained when the formulation is diluted with water, for example, to 2-500 l.
Claims (10)
(a)植物油又は鉱油あるいはこれらの油の混合物中に懸濁又は溶解された少なくとも1の雑草(grass)除草剤、ここで、当該除草剤は、以下の式(I):
(b)植物油又は鉱油あるいはこれらの油の混合物中に懸濁された少なくとも1のスルホニルウレア型の除草剤、及び
(c)少なくとも1の非イオン界面活性剤又はアニオン界面活性剤あるいは非イオン界面活性剤とアニオン界面活性剤の混合物、
を含む前記製剤。 A liquid herbicidal formulation,
(A) at least one grass herbicide suspended or dissolved in a vegetable oil or mineral oil or mixture of these oils, wherein the herbicide has the following formula (I):
(B) at least one sulfonylurea type herbicide suspended in a vegetable or mineral oil or mixture of these oils; and (c) at least one nonionic surfactant or anionic surfactant or nonionic surfactant. And a mixture of anionic surfactants,
Said formulation comprising:
Applications Claiming Priority (2)
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CH222298 | 1998-11-04 | ||
CH2222/98 | 1998-11-04 |
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JP2000579054A Division JP2002528471A (en) | 1998-11-04 | 1999-11-02 | Herbicide |
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JP2006232850A true JP2006232850A (en) | 2006-09-07 |
JP4800828B2 JP4800828B2 (en) | 2011-10-26 |
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ID=4228727
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JP2000579054A Withdrawn JP2002528471A (en) | 1998-11-04 | 1999-11-02 | Herbicide |
JP2006119643A Expired - Fee Related JP4800828B2 (en) | 1998-11-04 | 2006-04-24 | Herbicide |
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JP2000579054A Withdrawn JP2002528471A (en) | 1998-11-04 | 1999-11-02 | Herbicide |
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US (2) | US20020045549A1 (en) |
EP (1) | EP1126758A1 (en) |
JP (2) | JP2002528471A (en) |
KR (1) | KR100477180B1 (en) |
CN (1) | CN1325269B (en) |
AU (1) | AU760204B2 (en) |
BR (1) | BR9915001B1 (en) |
ID (1) | ID29430A (en) |
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JP2010524875A (en) * | 2007-04-18 | 2010-07-22 | シンジェンタ パーティシペーションズ アクチェンゲゼルシャフト | Pesticide composition that can be suspended in water |
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- 1999-11-02 CN CN99812950XA patent/CN1325269B/en not_active Expired - Fee Related
- 1999-11-02 KR KR10-2001-7005589A patent/KR100477180B1/en not_active IP Right Cessation
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JP2010524875A (en) * | 2007-04-18 | 2010-07-22 | シンジェンタ パーティシペーションズ アクチェンゲゼルシャフト | Pesticide composition that can be suspended in water |
Also Published As
Publication number | Publication date |
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ID29430A (en) | 2001-08-30 |
US20020045549A1 (en) | 2002-04-18 |
CN1325269B (en) | 2010-04-21 |
BR9915001A (en) | 2001-08-07 |
US20020193253A1 (en) | 2002-12-19 |
EP1126758A1 (en) | 2001-08-29 |
JP4800828B2 (en) | 2011-10-26 |
WO2000025586A1 (en) | 2000-05-11 |
US6673747B2 (en) | 2004-01-06 |
KR20010090815A (en) | 2001-10-19 |
CN1325269A (en) | 2001-12-05 |
JP2002528471A (en) | 2002-09-03 |
KR100477180B1 (en) | 2005-03-21 |
BR9915001B1 (en) | 2012-01-10 |
AU760204B2 (en) | 2003-05-08 |
AU1268600A (en) | 2000-05-22 |
MY124625A (en) | 2006-06-30 |
TW508217B (en) | 2002-11-01 |
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